Introduction: Cystic fibrosis (CF) is an inherited, progressive, multisystem disease. Better physical capacity may slow disease progression, thus improving prognosis and survival. The objective of this research was to evaluate the physical capacity of children admitted to the National CF Program of the Metropolitan Region, Chile. Patients and Method: A multicenter, cross-sectional study design was used. The inclusion criteria were children aged 6 to 12 years enrolled in the National CF Program; Tanner sexual maturity stage I, no respiratory exacerbations in the last 30 days, and no musculoskeletal pathologies. The maximum aerobic capacity was assessed through the peak oxygen uptake (VO2 peak) and determined with an incremental protocol in a magnetic cycle ergometer connected to an ergo-spirometer with which, at the same time, respiratory gases, oxygen consumption and carbon dioxide production values every 30 seconds, anaerobic threshold, and maximum workload were analyzed. The values of forced vital capacity (FVC), forced expiratory volume in 1 second (FEV1), FEV1/FVC ratio, and forced expiratory flows between 25% and 75% of vital capacity were assessed through ergo-spirometry. At the beginning of the ergo-spirometry, arterial oxygen saturation, respiratory rate, heart rate, blood pressure, tidal volume and the perception of lower extremity fatigue and dyspnea were recorded using the modified Borg scale. The test lasted approximately 10 minutes. Results: The clinical records of 43 children collected from six health centers were reviewed. Out of these, 29 children met inclusion criteria, and 23 were recruited. Two children were unable to participate, reducing the final subject group to 21 (13 males, 8 females). The mean age was 8.8 ± 2 years; weight 30.5 ± 10.9 kg; height 1.32 ± 0.11 m; and body mass index 17.1 ± 3.5 (z-score 0.01 ± 1.34). More than half of the children (61%) had normal weight. The obtained VO2 peak was 43.7 ± 6.5 ml/min/kg (106.7 ± 19.8% of the predictive values). Only 10% of the children had values lower than those predicted by sex and age. No correlations were found between VO2 peak and anthropometric and pulmonary function variables. Conclusion: Most of the evaluated children (90%) had physical capacity similar to healthy subjects by sex and age.

Additional Metadata
Keywords Children, Cystic fibrosis, Maximal oxygen uptake, Physical capacity
Persistent URL dx.doi.org/10.4067/S0370-41062018005000812, hdl.handle.net/1765/111911
Journal Revista Chilena de Pediatria
Citation
Puppo, H. (Homero), Von Oetinger, A. (Astrid), Benz, E. (Elizabeth), Torres-Castro, R. (Rodrigo), Zagolín, M. (Mónica), Boza, M.L. (María Lina), … Perillán, J. (José). (2018). Characterization of the physical capacity in children of the Chilean national program of cystic fibrosis. Revista Chilena de Pediatria, 89(5), 638–643. doi:10.4067/S0370-41062018005000812